The following data is part of a premarket notification filed by Puritan Bennett Corp. with the FDA for Pb 7200 Series Ventilatory System W/keyboard.
Device ID | K930017 |
510k Number | K930017 |
Device Name: | PB 7200 SERIES VENTILATORY SYSTEM W/KEYBOARD |
Classification | Ventilator, Continuous, Facility Use |
Applicant | PURITAN BENNETT CORP. 2200 FARADAY AVE. Carlsbad, CA 92008 |
Contact | Ann-marie Butler |
Correspondent | Ann-marie Butler PURITAN BENNETT CORP. 2200 FARADAY AVE. Carlsbad, CA 92008 |
Product Code | CBK |
CFR Regulation Number | 868.5895 [🔎] |
Decision | Se Subject To Tracking Reg (ST) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-01-04 |
Decision Date | 1994-09-22 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10884521130326 | K930017 | 000 |
20884521113678 | K930017 | 000 |
20884521113661 | K930017 | 000 |